Sodium Acetate → HCID 22065264, compound

HRID 1828071Notes

Reaction equation

HRID 1828071 reaction equation
[OH:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:21])[CH:10]([C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[C:15]([OH:20])[CH:14]=1)[CH2:11]Br.[C:22]([O-:25])(=O)[CH3:23].[Na+]>CO>[OH:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:21])[C:10]([C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[C:15]([OH:20])[CH:14]=1)=[CH2:11].[OH:8][C:6]1[CH:7]=[C:2]2[C:3]([C:9](=[O:21])[CH:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH:11]([C:4]3[CH:5]=[CH:23][C:22]([OH:25])=[C:2]([OH:1])[CH:3]=3)[O:1]2)=[CH:4][CH:5]=1

Participants

5

Conditions

Temperature
60 °C

Procedure

0.157 g of 1-(2,4-dihydroxyphenyl)-2-(3′,4′-dihydroxyphenyl)-1-oxo-3-bromo-propane, the major product of step 3 in Example 3, and about 2 molar equivalents of sodium acetate ware mixed with 88 mL of methanol and heated at about 60° C. for 4 hours. After cooling, the mixture was acidified to pH 5 and the methanol was removed under reduced pressure. Tile residue was dissolved in ethyl acetate (50 mL) and the solution was washed with water and concentrated. The crude product was separated by column chromatography to yield approximately equal amounts of 1-(2,4-dihydroxyphenyl)-2-(3′,4′-dihydroxyphenyl)-1-oxo-2-propene and 7-hydroxy-(3′,4′,-dihydroxyphenyl)-2,3-dihydroisoflavone.

Workup

  1. temperatureAfter cooling
  2. customthe methanol was removed under reduced pressure
  3. dissolutionTile residue was dissolved in ethyl acetate (50 mL)
  4. washthe solution was washed with water
  5. concentrationconcentrated
  6. customThe crude product was separated by column chromatography

Sources & evidence

ORD record
ord-58011fc31ef44b7185dcbd93f1fe6600
Source dataset
uspto-grants-2006_06
Patent number
US07056952B1

Reaction notes

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